A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384074



Internal ID21041627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174497001..174511700hg38UCSC Ensembl
chr4:175418152..175432851hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3814700
hg1914700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112453
Samples
Known GenesHPGD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384074
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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